Sébastien Feuillette - Publications

Affiliations: 
University of Rouen 

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Nicolas G, Sévigny M, Lecoquierre F, Marguet F, Deschênes A, Del Pelaez MC, Feuillette S, Audebrand A, Lecourtois M, Rousseau S, Richard AC, Cassinari K, Deramecourt V, Duyckaerts C, Boland A, et al. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics. Acta Neuropathologica Communications. 10: 20. PMID 35151370 DOI: 10.1186/s40478-022-01314-x  0.729
2021 Rovelet-Lecrux A, Feuillette S, Miguel L, Schramm C, Pernet S, Quenez O, Ségalas-Milazzo I, Guilhaudis L, Rousseau S, Riou G, Frébourg T, Campion D, Nicolas G, Lecourtois M. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathologica Communications. 9: 196. PMID 34922638 DOI: 10.1186/s40478-021-01294-4  0.679
2020 Feuillette S, Charbonnier C, Frebourg T, Campion D, Lecourtois M. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in . Frontiers in Neuroscience. 14: 68. PMID 32116515 DOI: 10.3389/Fnins.2020.00068  0.644
2017 Feuillette S, Delarue M, Riou G, Gaffuri AL, Wu J, Lenkei Z, Boyer O, Frébourg T, Campion D, Lecourtois M. Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations. Journal of Molecular Neuroscience : Mn. PMID 28429234 DOI: 10.1007/S12031-017-0908-Y  0.586
2012 Reinhardt A, Feuillette S, Cassar M, Callens C, Thomassin H, Birman S, Lecourtois M, Antoniewski C, Tricoire H. Lack of miRNA Misregulation at Early Pathological Stages in Drosophila Neurodegenerative Disease Models. Frontiers in Genetics. 3: 226. PMID 23115562 DOI: 10.3389/Fgene.2012.00226  0.335
2012 Miguel L, Avequin T, Delarue M, Feuillette S, Frébourg T, Campion D, Lecourtois M. Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila. Neurobiology of Aging. 33: 1008.e1-15. PMID 22118902 DOI: 10.1016/J.Neurobiolaging.2011.10.008  0.716
2011 Talmat-Amar Y, Arribat Y, Redt-Clouet C, Feuillette S, Bougé AL, Lecourtois M, Parmentier ML. Important neuronal toxicity of microtubule-bound Tau in vivo in Drosophila. Human Molecular Genetics. 20: 3738-45. PMID 21705366 DOI: 10.1093/Hmg/Ddr290  0.525
2010 Feuillette S, Deramecourt V, Laquerriere A, Duyckaerts C, Delisle MB, Maurage CA, Blum D, Buée L, Frébourg T, Campion D, Lecourtois M. Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains. Brain Research. 1345: 182-9. PMID 20460118 DOI: 10.1016/J.Brainres.2010.05.007  0.703
2010 Feuillette S, Miguel L, Frébourg T, Campion D, Lecourtois M. Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein. Journal of Neurochemistry. 113: 895-903. PMID 20193038 DOI: 10.1111/J.1471-4159.2010.06663.X  0.729
2009 Feuillette S, Deramecourt V, Laquerrière A, Blard O, Duyckaerts C, Delisle M, Maurage C, Frebourg T, Campion D, Lecourtois M. O1-6 Identification par crible génétique dans la drosophile de modulateurs de la neurotoxicité de la protéine Tau et caractérisation neuropathologique de leurs homologues humains Revue Neurologique. 165: 40. DOI: 10.1016/S0035-3787(09)72589-5  0.483
2007 Blard O, Feuillette S, Bou J, Chaumette B, Frébourg T, Campion D, Lecourtois M. Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila. Human Molecular Genetics. 16: 555-66. PMID 17309878 DOI: 10.1093/Hmg/Ddm011  0.665
2006 Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38: 24-6. PMID 16369530 DOI: 10.1038/Ng1718  0.677
2005 Feuillette S, Blard O, Lecourtois M, Frébourg T, Campion D, Dumanchin C. Tau is not normally degraded by the proteasome Journal of Neuroscience Research. 80: 400-405. PMID 15795929 DOI: 10.1002/Jnr.20414  0.681
2004 Dumanchin C, Feuillette S, Frebourg T, Campion D. P3-239 Tau is not degraded in vitro in SH5Y-SY human cells by the 26S proteasome under physiological conditions Neurobiology of Aging. 25: S423. DOI: 10.1016/S0197-4580(04)81389-7  0.557
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